Department of Chemical and Biomolecular Engineering, Faculty of Engineering, National University of Singapore, Singapore.
Nanotechnology. 2011 Sep 2;22(35):355401. doi: 10.1088/0957-4484/22/35/355401. Epub 2011 Aug 9.
A simple and scalable procedure combining hydrothermal synthesis with post-synthesis calcination was developed to produce a linker-free, thermally stable, mesoscale 3D ordered assembly of spinel-type ZnCo(2)O(4) nanocrystals. The mesoscale assembly with distinctively sharp edges was formed by close-packing the ZnCo(2)O(4) nanocrystal building blocks with a unit size changeable by the synthesis temperature. A self-templating mechanism based on the topotactic transformation of an oxalato-bridged precursor coordination compound was proposed for the assembly. The packaging of crystalline ZnCo(2)O(4) nanoparticles, an active lithium ion storage compound, into a dense organized structure is an effective way to increase the volumetric capacity of ZnCo(2)O(4) nanoparticles for reversible lithium ion storage. The highly ordered 3D assembly of ZnCo(2)O(4) demonstrated excellent reversible lithium ion storage properties and a specific capacity (∼800 mAh g(-1)) much higher than that of carbon (typically ∼ 350 mAh g(-1)).
开发了一种简单且可扩展的方法,将水热合成与后合成煅烧相结合,以生产无连接体、热稳定的尖晶石型 ZnCo(2)O(4)纳米晶的介观 3D 有序组装。通过紧密堆积 ZnCo(2)O(4)纳米晶构建块,形成具有独特锐边的介观组装体,其单元尺寸可以通过合成温度改变。提出了一种基于草酸桥连前体配位化合物的拓扑转变的自模板机制来解释该组装过程。将锂离子存储活性化合物结晶 ZnCo(2)O(4)纳米颗粒封装成致密的有序结构是提高 ZnCo(2)O(4)纳米颗粒可逆锂离子存储体积容量的有效方法。高度有序的 3D ZnCo(2)O(4)组装体表现出优异的可逆锂离子存储性能和比碳(通常约为 350 mAh g(-1))高得多的比容量(约 800 mAh g(-1))。